For information about a range of treatments, procedures and operations such as having tonsils and adenoids removed, grommets inserted, and anaesthetic. If your child is having a procedure, you might also find the section Coping with treatment and hospital useful.
When your child has a general anaesthetic, an anaesthetist will give them medicine to make them unaware and unconscious. You have an important role in preparing your child for their anaesthetic so that their experience is as positive as possible.
Scientists are developing stem cell therapies for the replacement or repair of damaged tissues such as nerves, muscle and other parts of the body. Doctors and scientists are researching stem cell therapy and looking at the best ways to use stem cells in cerebral palsy.
The aims of treatment for Crohn's disease are to control inflammation, relieve symptoms, make sure your child is growing well and has the vitamins and minerals they need. Some children may need to see a dietitian as part of their treatment.
A drip is a short, small plastic tube that a doctor or nurse will put into your child's vein, using a needle. They will leave a plastic tube in so that fluids and medicines go directly into your child's blood.
A morphine infusion is pain relieving medicine your child receives continuously through a pump. Children usually have it after an operation but can sometimes have it to manage pain that results from a medical condition.
PCA stands for patient controlled analgesia. A PCA pump is a device that allows your child to give themselves a pre-set amount of pain medicine (usually morphine), as needed, by pressing a hand-held button.
Tongue tie is a condition that involves a small piece of tissue connecting the tongue to the bottom of the mouth. This is called the frenulum. When a baby's frenulum is short or tight it can stop their tongue from moving properly. This is called a tongue tie. Tongue tie may cause a problem with breastfeeding for some babies.
Tube feeding generally involves delivering a liquid feed through the nose (nasal tube) or stomach (gastrostomy tube). Tube feeding helps your child to meet their nutritional needs when they are not able to eat or drink enough by mouth.
A general guide, to support your child progressing to oral feeding. Make sure you discuss this with your health professional, who knows your child well. Your health professional will help you to create a plan for your child.
The aims of treatment for ulcerative colitis are to control inflammation, relieve symptoms, make sure your child is growing well and has the vitamins and minerals they need. Some children may need to see a dietitian as part of their treatment.